Proteinové signální dráhy řídící diferenciaci nervových kmenových buněk

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985904%3A_____%2F08%3A00313817" target="_blank" >RIV/67985904:_____/08:00313817 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Protein signaling pathways in differentiation of neural stem cells

Popis výsledku v původním jazyce

Neural stem cells (NSC) are promising source of cells for the treatment of central nervous system diseases. Access to regulatory signaling proteins present in low copies has been very restrictive until now due to scarcity of stem cell populations. Hence,we utilized the KinexTM Antibody Microarray analysis where profiles of the proliferating porcine NSC and differentiated counterparts were compared. Selected changes were verified by immunoblotting. Differentiated neural cells exhibited an increased level of RafB kinase, MAPKK 3, heme oxygenase 2 (HO2) and protein phosphatase 4C. In contrast, for the NSC were typical high level of G protein-coupled receptor-serine kinase 2 and enhanced phosphorylations of B-crystallin (S45), PKC (T655), PKC (S738/S742)together with eIF2 (S51). Immunocytochemistry confirmed expression profiles and intense cytoplasmic localization of HO2 in neurons but a weaker signal in glia. Phospho-S45 B-crystallin was localized in nuclei of differentiated cells.

Název v anglickém jazyce

Protein signaling pathways in differentiation of neural stem cells

Popis výsledku anglicky

Neural stem cells (NSC) are promising source of cells for the treatment of central nervous system diseases. Access to regulatory signaling proteins present in low copies has been very restrictive until now due to scarcity of stem cell populations. Hence,we utilized the KinexTM Antibody Microarray analysis where profiles of the proliferating porcine NSC and differentiated counterparts were compared. Selected changes were verified by immunoblotting. Differentiated neural cells exhibited an increased level of RafB kinase, MAPKK 3, heme oxygenase 2 (HO2) and protein phosphatase 4C. In contrast, for the NSC were typical high level of G protein-coupled receptor-serine kinase 2 and enhanced phosphorylations of B-crystallin (S45), PKC (T655), PKC (S738/S742)together with eIF2 (S51). Immunocytochemistry confirmed expression profiles and intense cytoplasmic localization of HO2 in neurons but a weaker signal in glia. Phospho-S45 B-crystallin was localized in nuclei of differentiated cells.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

EB - Genetika a molekulární biologie

OECD FORD obor

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Projekt

<a href="/cs/project/1M0538" target="_blank" >1M0538: Centrum buněčné terapie a tkáňových náhrad</a><br>

Návaznosti

Z - Vyzkumny zamer (s odkazem do CEZ)

Rok uplatnění

2008

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Proteomics

ISSN

1615-9853

e-ISSN

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Svazek periodika

8

Číslo periodika v rámci svazku

-

Stát vydavatele periodika

DE - Spolková republika Německo

Počet stran výsledku

13

Strana od-do

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Kód UT WoS článku

000261003800015

EID výsledku v databázi Scopus

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